Principal Scientist - Toxicology Project Team Representative

Posted:
8/18/2024, 5:00:00 PM

Experience Level(s):
Senior

Field(s):
Product

Workplace Type:
Remote

Career Category

Research

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

Principal Scientist - Toxicology Project Team Representative

Live

What you will do

Let’s do this. Let’s change the world. Amgen is seeking a talented individual to provide scientific leadership and play an active role in the process of drug development from late-stage discovery through marketed products. Working in a collaborative team environment, in this vital role you will contribute to the safety assessment of small molecule and biologic therapeutics by synthesis of existing knowledge and comprehensive investigations of toxicological activity. Amgen toxicologists make significant contributions to multiple teams, work in multiple therapeutic areas, and mentor and motivate other staff members.

Responsibilities include:

  • Participate and contribute toxicology, safety and other subject matter expertise to key project teams. Provide regular updates as appropriate to project teams and management.
  • As a project team representative, will design, implement, manage and analyze safety assessment programs in support of drug development candidates.
  • Responsible for originating novel protocols to solve experimental questions and devising strategies/planning activities to achieve project goals.
  • Will critically evaluate and interpret results of scientific experiments and contribute to appropriate sections of internal governance documents, INDs, BLAs, NDAs and other regulatory documents.
  • Coordinate and collaborate with other Amgen scientists and external organizations in facilitating research projects.
  • May participate in licensing and due diligence activities.
  • May mentor other Amgen staff for implementation and oversight of studies supporting research and development programs.
  • May represent Amgen's nonclinical safety issues at national and international regulatory meetings. May participate in external industry initiatives to improve drug safety assessment paradigms.

Basic Qualifications:

Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 2 years of Toxicology, Pathology, Life Sciences or a related field

Or

Master’s degree and 5 years of Toxicology, Pathology, Life Sciences or a related field experience

Preferred Qualifications:

  • A minimum of 5 years post-PhD or 12 years post Master’s degree of Pharmaceutical and/or Biotechnology industry experience is preferred.
  • Experience leading toxicology research programs supporting safety assessment of drug development candidates is preferred
  • Experience in the preparation of regulatory documents and interactions with US and international regulatory agencies.
  • Board certification in Toxicology is preferred.
  • Excellent written and verbal communication skills and the ability to work independently and to build productive cross-functional collaborations both internally and externally are essential.
  • Working understanding of cutting edge science and technology being used to enhance investigation of drug development safety issues.
  • National and international recognition as a field expert.

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans and bi-annual company-wide shutdowns
  • Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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Salary Range

143,100.00 USD - 169,473.00 USD

Amgen

Website: https://amgen.com/

Headquarter Location: Thousand Oaks, California, United States

Employee Count: 10001+

Year Founded: 1980

IPO Status: Public

Last Funding Type: Post-IPO Debt

Industries: Biotechnology ⋅ Health Care ⋅ Manufacturing ⋅ Pharmaceutical